Canonical Allele Identifier: CA343983836

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712699T>A (hg19) ; chr1:g.196743569T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743569T>A , CM000663.2:g.196743569T>A	GRCh38
NC_000001.10:g.196712699T>A , CM000663.1:g.196712699T>A	GRCh37
NC_000001.9:g.194979322T>A	NCBI36
NG_007259.1:g.96559T>A , LRG_47:g.96559T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4279T>A
ENST00000695970.1:c.3077T>A	ENSP00000512297.1:p.Phe1026Tyr
ENST00000695971.1:c.3230T>A	ENSP00000512298.1:p.Phe1077Tyr
ENST00000695972.1:c.*328T>A	ENSP00000512299.1:n.*328T>A
ENST00000695973.1:c.*1615T>A	ENSP00000512300.1:n.*1615T>A
ENST00000695974.1:c.3074T>A	ENSP00000512301.1:p.Phe1025Tyr
ENST00000695975.1:c.*1378T>A	ENSP00000512302.1:n.*1378T>A
ENST00000695976.1:c.3062T>A	ENSP00000512303.1:p.Phe1021Tyr
ENST00000695981.1:c.3251T>A	ENSP00000512306.1:p.Phe1084Tyr
ENST00000695984.1:c.1259T>A	ENSP00000512309.1:p.Phe420Tyr
ENST00000695986.1:c.*2902T>A	ENSP00000512311.1:n.*2902T>A
ENST00000696026.1:c.*1533T>A	ENSP00000512335.1:n.*1533T>A
ENST00000696027.1:c.3245T>A	ENSP00000512336.1:p.Phe1082Tyr
ENST00000696028.1:c.3179T>A	ENSP00000512337.1:p.Phe1060Tyr
ENST00000696029.1:c.3245T>A	ENSP00000512338.1:p.Phe1082Tyr
ENST00000696031.1:c.*2769T>A	ENSP00000512340.1:n.*2769T>A
ENST00000696032.1:c.3251T>A	ENSP00000512341.1:p.Phe1084Tyr
ENST00000696033.1:c.1160-36228T>A	ENSP00000512342.1:n.1160-36228T>A
ENST00000367429.9:c.3251T>A MANE Select	ENSP00000356399.4:p.Phe1084Tyr
ENST00000367429.8:c.3251T>A	ENSP00000356399.4:p.Phe1084Tyr
ENST00000466229.5:n.6349T>A
NM_000186.3:c.3251T>A , LRG_47t1:c.3251T>A	NP_000177.2:p.Phe1084Tyr
XR_001737134.2:n.3437T>A
NM_000186.4:c.3251T>A MANE Select	NP_000177.2:p.Phe1084Tyr